Canonical Allele Identifier: CA374037742

Gene: BICD2

Linked Data

• dbSNP Id: rs764409038
• gnomAD v3: 9-92719147-C-A
• gnomAD v4: 9-92719147-C-A
• MyVariant Identifiers: chr9:g.95481429C>A (hg19) ; chr9:g.92719147C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92719147C>A , CM000671.2:g.92719147C>A	GRCh38
NC_000009.11:g.95481429C>A , CM000671.1:g.95481429C>A	GRCh37
NC_000009.10:g.94521250C>A	NCBI36
NG_033908.1:g.50655G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1498G>T MANE Select	ENSP00000349351.6:p.Ala500Ser
ENST00000356884.10:c.1498G>T	ENSP00000349351.6:p.Ala500Ser
ENST00000375512.3:c.1498G>T	ENSP00000364662.3:p.Ala500Ser
NM_001003800.1:c.1498G>T	NP_001003800.1:p.Ala500Ser
NM_015250.3:c.1498G>T	NP_056065.1:p.Ala500Ser
XM_017014551.1:c.1579G>T	XP_016870040.1:p.Ala527Ser
NM_001003800.2:c.1498G>T MANE Select	NP_001003800.1:p.Ala500Ser
NM_015250.4:c.1498G>T	NP_056065.1:p.Ala500Ser